SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.

Source:http://linkedlifedata.com/resource/pubmed/id/17656375

Hum. Mol. Genet. 2007 Oct 15 16 20 2482-93

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PMID
17656375